融入WTO——为农业服务的化工矿产资源发展战略构想

我国直接为农业服务的磷、硫、钾矿资源总体形势不容乐观。针对各自资源特点,应采取不同的发展战略:磷——立足国内,有进有出,南出北进;硫——立足国内,适当进口,调整结构,必要储备;钾——稳定进口,国外开发,国内开发,国内找矿,四位一体,分三步走。为此建议:将磷、硫、钾纳入战略性矿产资源的范畴进行管理和规划;强化地勘队伍,加大找矿力度;增加投入,寻求新的突破;加大“走出去”的步伐;规范进出口秩序;国家在更高的层面进行宏观调控;拓宽为农业服务的新领域。     

阿尔泰地区铜镍矿床综合信息找矿模型及成矿预测

阿尔泰地区存在 5条与深大断裂有关的基性、超基性岩带 ,是铜镍硫化物矿床产出的有利地段 ,其中喀拉通克铜镍矿是我国大型铜镍矿之一。通过对成矿必要条件的深入研究 ,得出深大断裂及其次级断裂控制了岩体的产出 ,北北西向断裂叠加北西向断裂控制了矿体的产出 ;成矿充分条件是基性、超基性岩体 ,总结了岩体含矿性的评价指标。结合重磁及地化资料 ,在喀拉通克铜镍矿的成矿模式基础上 ,建立了区域综合信息找矿模型 ,进行成矿预测 ,圈定靶区 9处。     

青海驼路沟钴(金)矿床成矿物质来源的黄铁矿氦氩硫铅同位素示踪

为查明青海驼路沟新型独立钴(金)矿床的成因和成矿物质来源,文章对矿区发育的块状、条带状和浸染状黄铁矿矿石进行了黄铁矿流体包裹体氦氩同位素和黄铁矿硫、铅同位素测试。结果表明,不同类型矿石的成矿流体氦、氩同位素组成基本一致,3He/4He介于0.10~0.31Ra(平均0.21Ra),40Ar/36Ar比值为302~569(平均373),反映钴矿化流体主要来源于在赋矿岩系中深循环的大气降水;矿石黄铁矿硫同位素值分布集中且接近于零,δ34S变化于-4.5‰~+1.5‰,集中在-1.8‰~-0.2‰,显示深部来源;矿石铅以高放射性成因为特征(206Pb/204Pb>19.279、207Pb/204Pb>15.691、208Pb/204Pb>39.627),且自地层围岩→区域早古生代火山岩→矿石依次明显增大,可能指示高放射性成因矿石铅主要是由以深循环大气降水来源为主的热液不断从围岩地层中淋取而来。     

四川巴塘夏塞花岗岩和银多金属矿床年龄及ち颉⑶ν位素组成

为了解四川西部夏塞银多金属矿区黑云母二长花岗岩形成和矿化发生的时代及成矿物质来源,测定了该矿区绒依措和若洛隆花岗岩的Rb_Sr年龄和钾长石、黑云母及主要银矿化阶段石英的40Ar/39Ar年龄及矿石的硫、铅同位素组成。花岗岩的结晶年龄约为93Ma,银矿化年龄约为75Ma。矿石硫可能源于花岗岩,但不能排除源于弱沉积围岩的可能性;矿石、花岗岩和弱变质沉积围岩的铅同位素组成相似,铅主要源于上地壳,少量源于下地壳。     

胶东金矿集区硫和碳的循环与控矿作用

胶东金矿集区矿石中普遍含金属硫化物和碳酸盐矿物,某些矿床中还见有富含炭质的断裂破碎带.成矿溶液中含有大量的SO4^2-、HCO3^-、CO2和有机质等的含硫和含碳组分.矿石硫同位素组成明显富集重硫,结合胶东金矿主要成矿时期（早白垩世）特殊的地质背景、同期海水硫酸盐δ^34S平均值（约＋16‰）及现代海水沿NE-NNE向断裂倒灌情况,笔者认为,硫的主要来源与海水硫的大量补给有关.而根据碳、氧同位素组成特征分析,形成金矿床中方解石的物源有很大一部分来自前寒武系碳酸盐岩.浅表环境下成矿金属元素及硫、碳等物质在热液对流系统中的大规模循环是成矿的关键,SO4^2-与S2^-之间的临界转化是制约成矿金属元素活化-迁移-聚集的重要因素,而含碳组分（CO3^2-、HCO3^-、CO2和有机质）则有利于Au、Cu、Pb、Zn等元素的活化和迁移,含硫和含碳组分的循环及有关的物理化学反应之间有明显的关联性.     

粤北大宝山多金属矿床成矿流体的He-Ar-Pb-S同位素示踪

大宝山多金属矿床是粤北地区典型的巨厚型及细脉带型矿化的多金属硫化物矿床.层状和脉状黄铁矿的氦氩同位素表明:3He/4He的R/Ra值为0.60～4.13,40Ar/86Ar=327～411,反映该成矿流体是大气饱和水(海水)与地幔流体混合作用的结果.铅和硫同位素都揭示了层状(块状)和脉状矿体可能来自不同时期的成矿流体.其中层状矿体为泥盆纪海底火山喷发沉积作用所致,脉状矿体可能来自燕山期岩浆热液充填叠加形成,古大陆碎屑物质和部分有机质的还原对后期成矿流体具有较大的影响作用.     

The Atmospheric Oxidation of the HS Radical: Reaction with NO2

The atmospheric reaction between HS and NO₂ was theoretically investigated at 298 K and 1 atm of pressure. Our results show that the first reaction step will lead to the formation of HSNO₂ or HSONO, spontaneously and exothermically. HSONO easily decomposes into HSO + NO. On the other hand, HSNO₂ can hardly dissociate in the reactants, and its isomerization to other adducts is much hindered. Production of HNO + SO and SNO + OH was found to be unfavorable. Thus, the main products would be HSO + NO and HSNO₂, and new investigations focusing on the atmospheric fate of HSNO₂ are suggested. A general discussion of the fate of HS under atmospheric conditions is presented. Recent investigations indicate that NO₂, O₂ and N₂O should be the most important oxidants of HS, while the O₃ influence will not be significant.     

热解硫酸钡制备硫同位素分析试样二氧化硫

改进了硫同位素分析中由ＢａＳＯ４制备ＳＯ２的方法：ＢａＳＯ４和Ｖ２Ｏ５及ＳｉＯ２混合后覆盖铜丝,在真空状态９８０℃加热２０ｍｉｎ,用液氮捕集ＳＯ２。与火焰直接加热分解法相比,用高温炉方便,改善了制样环境,避免污染。经国际标样和国家标准物质分析验证,结果与标准值相符,标准偏差（１σ）在±００９‰～±０２０‰,符合分析要求。     

A Three-Dimensional Global Model Study of Carbonyl Sulfide in the Troposphere and the Lower Stratosphere

Global distributions of carbonyl sulfide and carbon disulfide have been calculated with a three-dimensional global model of the atmospheric general circulation (ECHAM). The model calculates a global sink strength for carbonyl sulfide of 0.3 Tg S yr^-1, with vegetation uptake being the largest sink. With this sink strength, the sources have to be close to the lower limit of the present estimate in the literature. The calculated mixing ratios are higher in the Southern Hemisphere than in the Northern Hemisphere. This interhemispheric gradient is the opposite of what is observed demonstrating that the present knowledge of the distribution of sinks and sources is not fully adequate. The model calculations support the idea that the open oceans could act as a net sink of carbonyl sulfide. The calculated stratospheric photolysis of carbonyl sulfide constitutes about 4% of the total sink of carbonyl sulfide. A stratospheric production of sulfate from carbonyl sulfide of 0.013 Tg S yr^-1 is obtained, which is 3 to 12 times less than what is needed to maintain the stratospheric sulfate aerosol layer. Although these results are associated with uncertainties, due to the low upper boundary and coarse vertical resolution of the model, they support recent findings of a low stratospheric production of sulfate from carbonyl sulfide. Instead, sulfur dioxide transported from the troposphere is calculated to be the most important precursor for the stratospheric sulfate aerosol layer.     

Model Simulations on the Variability of Particulate MSA to Non-Sea-Salt Sulfate Ratio in the Marine Environment

A box model was constructed to investigate connections between the particulate MSA to non-sea-salt sulfate ratio, R, and DMS chemistry in a clean marine boundary layer. The simulations demonstrated that R varies widely with particle size, which must be taken into account when interpreting field measurements or comparing them with each other. In addition to DMS gas-phase chemistry, R in the submicron size range was shown to be sensitive to the factors dictating sulfate production via cloud processing, to the removal of SO₂ from the boundary layer by dry deposition and sea-salt oxidation, to the entrainment of SO₂ from the free troposphere, to the relative concentration of sub- and supermicron particles, and to meteorology. Three potential explanations for the increase of R toward high-latitudes during the summer were found: larger MSA yields from DMS oxidation at high latitudes, larger DMSO yields from DMS oxidation followed by the conversion of DMSO to MSA at high latitudes, or lower ambient H₂O₂ concentrations at high latitudes leading to less efficient sulfate production in clouds. Possible reasons for the large seasonal amplitude of R at mid and high latitudes include seasonal changes in the partitioning of DMS oxidation to the OH and NO₃ initiated pathways, seasonal changes in the concentration of species participating the DMS-OH reaction pathway, or the existence of a SO₂ source other than DMS oxidation in the marine boundary layer. Even small anthropogenic perturbations were shown to have a potential to alter the MSA to non-sea-salt sulfate ratio.